|Publication number||US6444860 B2|
|Application number||US 09/750,748|
|Publication date||Sep 3, 2002|
|Filing date||Dec 29, 2000|
|Priority date||Feb 17, 1999|
|Also published as||CA2363542A1, CN1339031A, DE60002175D1, EP1153021A1, EP1153021B1, US6210608, US20010039356, WO2000049010A1|
|Publication number||09750748, 750748, US 6444860 B2, US 6444860B2, US-B2-6444860, US6444860 B2, US6444860B2|
|Inventors||You-Ping Chan, Patrick Jean|
|Original Assignee||Corning S.A.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (19), Classifications (26), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present application is a division of U.S. patent application Ser. No. 09/504,689, filed Feb. 16, 2000, now U.S. Pat. No. 6,210,608.
The present invention relates to novel annelated naphthopyran- or phenanthropyran-type compounds which have, in particular, photochromic properties. The invention also relates to photochromic compositions and photochromic ophthalmic articles (lenses for example) which contain said naphthopyrans or phenanthropyrans. The invention also covers the preparation of these novel compounds.
The photochromic compounds are capable of changing colour under the influence of a poly- or mono-chromatic light (UV for example) and of returning to their initial colour when the luminous irradiation ceases, or under the influence of temperature and/or a poly- or mono-chromatic light different from the first.
The photochromic compounds find applications in various fields, e.g. for the manufacture of ophthalmic lenses, contact lenses, solar protection glasses, filters, camera optics or photographic apparatus optics or other optical devices and observation devices, glazing, decorative objects, bill elements or even for information storage by optical inscription (coding).
In the field of ophthalmic optics, and in particular the spectacles trade, a photochromic lens which comprises one or more photochromic compounds must have:
a high transmission in the absence of ultraviolets,
a low transmission (high colourability) under solar irradiation,
adapted coloration and discoloration kinetics,
a tint acceptable to the consumer (grey or brown preferably) with preferably a maintenance of the chosen tint during the coloration and the discoloration of the lens,
a maintenance of the performances, the properties, within a temperature range of 0-40° C.,
a significant durability, since these objectives sought after are sophisticated corrective lenses and therefore expensive.
These lens characteristics are in fact determined by the active photochromic compounds which they contain; compounds which must furthermore be perfectly compatible with the organic or inorganic support which constitutes the lens.
Moreover, it is to be noted that obtaining a grey or brown tint may necessitate the use of at least two photochromes of different colours, i.e. having distinct maximal absorption wavelengths in the visible. This combination further imposes other requirements of the photochromic compounds. In particular, the coloration and discoloration kinetics of the (two or more) combined active photochromic compounds must be essentially identical. The same applies for their stability with time and also for their compatibility with a plastic or inorganic support.
Amongst the numerous photochromic compounds described in the prior art, benzopyrans and naphthopyrans may be cited which are described in patents or U.S. patent applications Ser. Nos. 3,567,605, 3,627,690, 4,826,977, 5,200,116, 5,238,981, 5,411,679, 5,429,744, 5,451,344, 5,458,814, 5,651,923, 5,645,767, 5,698,141, 5,783,116, WO-A-95 05382, FR-A-2,718,447, WO-A-96 14596, WO-A-97 21698 which are of the reduced formulae below:
The U.S. Pat. No. 5,651,923 patent notably claims the general structure below:
in which ring A, annelated with side f, is a benzothieno-, benzofurano- or indolo-type heterocycle.
The U.S. Pat. No. 5,783,116 patent describes more specifically naphthopyrans of the following general structure:
These compounds claim to satisfy the specifications defined above. In reality, if these compounds really do have one or more of the basic properties sought after, such as a high transmission in the absence of ultraviolets and a high colourability under solar irradiation, none of the compounds described hitherto have the complete combination of the properties sought after which are necessary for the production of satisfactory articles. In particular, none of these compounds is intrinsically grey or brown and the necessity of using an additional photochrome in order to obtain one of these two tints does subsist.
In this context, it is to the credit of the inventors for having been interested in this type of derivative as a base for developing novel photochromes, and for having proposed a novel family of molecules which have particularly advantageous photochromic properties.
Thus, according to a first of its aspects, the present invention relates to compounds of formula (I):
R1 and R2, which are identical or different, represent, independently:
a linear or branched alkyl group comprising 1 to 12 carbon atoms,
a cycloalkyl group comprising 3 to 12 carbon atoms,
an aryl or heteroaryl group comprising in its basic structure 6 to 24 carbon atoms or 4 to 24 carbon atoms respectively and at least one heteroatom selected from sulphur, oxygen and nitrogen; said basic structure being optionally substituted with at least one substituent selected from the whole of the substituents given below:
a halogen, and notably fluorine, chlorine and bromine,
a linear or branched alkyl group comprising 1 to 12 carbon atoms,
a linear or branched alkoxy group comprising 1 to 12 carbon atoms,
a haloalkyl or haloalkoxy group corresponding to the (C1-C12) alkyl or alkoxy groups above respectively which are substituted with at least one halogen atom, and notably a fluoroalkyl group of this type,
a linear or branched alkenyl group comprising 2 to 12 carbon atoms, and notably a vinyl group or an allyl group,
an —NH2 group,
an —NHR group, R representing a linear or branched alkyl group comprising 1 to 6 carbon atoms,
group, R′ and R″, which are identical or different, representing independently a linear or branched alkyl group comprising 1 to 6 carbon atoms or representing together with the nitrogen atom to which they are bound a 5- or 7-membered ring which can comprise at least one other heteroatom selected from oxygen, sulphur and nitrogen, said nitrogen being optionally substituted with an R′″ group, which is a linear or branched alkyl group comprising 1 to 6 carbon atoms,
a methacryloyl group or an acryloyl group,
an aralkyl or heteroaralkyl group, the alkyl group, which is linear or branched, comprising 1 to 4 carbon atoms and the aryl part of which has the same definition as that given supra for the aryl and heteroaryl group;
said two substituents R1 and R2 together form an adamantyl, norbornyl, fluorenylidene, di(C1-C6)alkylanthracenylidene or spiro(C5-C6)cycloalkylanthracenylidene group; said group being optionally substituted with at least one of the substituents listed above for R1, R2: an aryl or heteroaryl group;
R3, which are identical or different, represent, independently:
a halogen, and notably fluorine, chlorine or bromine,
a linear or branched alkyl group comprising 1 to 12 carbon atoms (advantageously 1 to 6 carbon atoms),
a cycloalkyl group comprising 3 to 12 carbon atoms,
a linear or branched alkoxy group comprising 1 to 12 carbon atoms (advantageously 1 to 6 carbon atoms),
a haloalkyl, halocycloalkyl, or haloalkoxy group corresponding to the alkyl, cycloalkyl, alkoxy groups above respectively, which are substituted with at least one halogen atom, notably selected from fluorine, chlorine and bromine,
an aryl or heteroaryl group having the same definition as that given supra for R1, R2,
an aralkyl or heteroaralkyl group, the alkyl group, which is linear or branched, comprising 1 to 4 carbon atoms, and the aryl and heteroaryl groups having the same definitions as those given supra for R1, R2,
an amine or amide group: —NH2, —NHR, —CONH2, —CONHR,
R, R′, R″ having their respective definitions given supra for the amine substituents of the values R1, R2: aryl or heteroaryl,
an —OCOR6 or —COOR6 group, R6 representing a straight or branched alkyl group comprising 1 to 6 carbon atoms, or a cycloalkyl group comprising 3 to 6 carbon atoms, or a phenyl group, optionally substituted with at least one of the substituents listed above for the values of R1, R2: aryl or heteroaryl;
at least two of the R3 groups, which are adjacent, form a 5- to 6-membered aromatic or non-aromatic ring which can comprise at least one heteroatom selected from the group comprising: oxygen, sulphur or nitrogen and/or at least one substituent selected from a C1-C6 alkyl group which is linear or branched, a C1-C6 alkoxy group which is linear or branched, and an amine group of formula —NH2, —NHR or
as defined above, as substituent, of the basic structure of the aryl or heteroaryl group representing R1 or R2;
m is an integer of 0 to 4;
R4, which are identical or different, represent, independently:
a halogen, preferably selected from the group comprising fluorine, chlorine and bromine,
or a C1-C6 alkyl group which is linear or branched;
n is an integer of 0 to 4.
The person skilled in the art will obviously have understood that the branched alkyl, alkoxy and alkenyl groups, as defined above, comprise a sufficient number of carbon in order to be branched (i.e. more than 3, more than 3, and more than 4 carbon atoms respectively).
The compounds of the invention—naphthopyrans or phenanthropyrans of formula (I)—have a high colourability, even at 40° C., combined with discoloration kinetics which are adapted to the applications sought after. The colours, which may be attained easily, vary from orange to blue.
Amongst said compounds of the invention, preferred are those which have the formula (I) in which:
R1, R2 are identical or different and represent independently optionally substituted aryl or heteroaryl groups the basic structure of which is selected from the group comprising phenyl, naphthyl, biphenyl, pyridyl, furyl, benzofuryl, dibenzofuryl, N-(C1-C6)alkylcarbazole, thienyl, benzothienyl, dibenzothienyl and julolidinyl groups; R1 and/or R2 representing, advantageously, a para-substituted phenyl group;
R1 and R2 together form an adamantyl or norbornyl group.
According to a first embodiment of the invention, the compounds (I) are such that at least two of their adjacent R3 substituents do not together form a ring.
According to a second embodiment of the invention, the compounds (I) are such that they comprise at least two adjacent R3 groups which together form an annelated carbocycle or heterocycle, which is optionally substituted (with a C1-C6 alkyl or alkoxy group, or with an amine group).
According to a variant of this second embodiment, the invention relates to the following phenanthrene structures of formulae (I.1) and (I.2):
in which R1, R2 and R4 are as defined above; R31 and R32 represent, independently, a group having the same definition as that given supra for R3 in the generic formula (I) which includes the two embodiments described above; R5 represents an alkyl, alkoxy or amine group as defined above, and m=0, 1, 2, n=0 to 4 and o=0 to 4.
In accordance with an interesting provision of the invention, notably in accordance with the two above-mentioned embodiments proper, n=0 in formulae (I), (I.1) or (I.2).
According to a second of its aspects, the present invention relates to a method of preparing the compounds (I), characterized in that it essentially consists in carrying out a condensation:
of at least one of the intermediate products of formulae (II.1), (II.2), (II.3) given below:
in which R3, R31, R32, R4, R5, m, n and o are as defined above with reference to formulae (I), (I.1), (I.2);
with at least one derivative of propargylic alcohol having formula (III) below:
in which R1 and R2 are as defined supra with reference to formula (I);
the condensation (II)/(III) being carried out advantageously in the presence of a catalyst, this catalyst being preferably selected from the group comprising para-toluenesulphonic acid, dodecylsulphonic acid or bromoacetic acid;
with at least one aldehyde derivative, having formula (III′) below:
in which R1 and R2 are as defined supra with reference to formula (I);
the condensation (II)/(III′) being carried out, advantageously, in the presence of a metallic complex, preferably a complex of titanium, titanium (IV) ethoxide being particularly preferred.
In practice, the condensation reaction between compounds (II) and (III′) can take place in solvents such as toluene, xylene or tetrahydrofuran, to which appropriate catalysts are optionally added. For more details on the condensation of compounds (II), (III′), reference may be made to the EP-A-0 562 915 patent application.
The compounds of formula (III) are known to the person skilled in the art and are obtained from the corresponding ketone according to a method described notably in the WO-A-96 14596 patent application. The ketone is itself commercial or is prepared according to the known methods such as the Friedel Crafts method (cf. WO-A-96 14596 and cited references).
Aldehydes (III′), which are derivatives of (III), are obtained by rearrangement in an acid medium (cf. J. Org. Chem., 1977, 42, 3403).
The compounds of formula (II) are obtained according to a synthetic scheme the various steps of which are adaptations of known methods. The preferred general synthetic schemes are given below, for compound (II.1). The compounds of formula (II.2) and (II.3) can be obtained by the same routes starting from the organomagnesium reagent of 2-bromo or 1-bromonaphthalene respectively.
Concerning route A, step 1 is carried out according to a method described by Basavaiaiah et al. (Tetrahedron Asymm. 1994, 5, 223-234), step 2 by Corey et al. (Tetrahedron Lett. 1975, 2647) and step 3 by Sepiol et al. (Synthesis 1979, 290). Concerning route B, step 1 is carried out according to a method described by Schoenleber et al. (WO-A-96 38435) and steps 2 and 3 according to Lin (U.S. Pat. No. 5,783,116).
According to a third of its aspects, the invention also relates to the novel intermediate products of formulae (II.1), (II.2), (II.3) recalled below:
in which R3, R31, R32, R4, R5, m, n and o are as defined supra with reference to formulae (I), (I.1) and (I.2).
The naphthopyrans or phenanthropyrans of the invention are obtained by the condensation of at least one compound having a formula type (II) (with a compound of formula III or III′).
According to a fourth of its aspects, the object of the invention is (co)polymer(s) and/or reticulate(s) obtained by polymerising and/or cross-linking at least one monomer consisting of a compound (I) as defined above. Thus, the compounds (I) according to the invention can be per se (co)monomers and/or be comprised in (co)polymerisable and/or crosslinkable (co)monomers. The (co)polymers and/or reticulates thus obtained can constitute photochromic matrices such as those presented infra.
According to a fifth of its aspects, the present invention relates to the use of said compounds of formula (I) of the invention as photochromic agents. Another object of the invention is, therefore:
firstly, novel photochromic compounds which are constituted by the naphthopyran or phenanthropyran derivatives such as defined above, taken alone or in a mixture of themselves and/or with at least one other photochromic compound of another type and/or with at least one non-photochromic colouring agent;
secondly, novel photochromic compositions which comprise at least one compound (I) as defined above, and/or one of its derivatives, and/or at least one linear or cross-linked (co)polymer containing at least one compound (I) according to the invention in its structure. Such photochromic compositions can contain at least one other photochromic compound, of another type and/or at least one non-photochromic colouring agent and/or at least one stabilising agent. These photochromic compounds of another type, non-photochromic colouring agents, and stabilising agents are prior art products known to the person skilled in the art.
Within the context of the present invention, combinations of photochromic compounds of the invention and/or combinations of photochromic compounds of the invention and photochromic compounds of another type according to the prior art are particularly recommended; such combinations being interesting in that they are suitable for generating grey or brown tints, which are desired by the public in applications such as ophthalmic spectacles or solar spectacles. These additional photochromic compounds can be those known to the person skilled in the art and described in the literature, e.g. chromenes (U.S. Pat. No. 3,567,605, U.S. Pat. No. 5,238,981, WO-A-94 22850, EP-A-0 562 915), spiropyrans or naphthospiropyrans (U.S. Pat. No. 5,238,981) and spiroxazines (Crano et al., “Applied Photochromic Polymer Systems”, Ed. Blackie & Son Ltd, 1992, chapter 2).
Said compositions according to the invention can also comprise:
non-photochromic colouring agents which enable adjusting the tint,
and/or one or more stabilising agents, such as an antioxidising agent for example,
and/or one or more anti-UV,
and/or one or more anti-radicals,
and/or one or more photochimic excited state deactivators.
These additives can notably enable improving the durability of said compositions.
The compounds of the invention envisaged within the context of their photochromic applications can be used in solution. Thus, a photochromic solution can be obtained by dissolving at least one of said compounds in an organic solvent such as toluene, dichloromethane, tetrahydrofuran or ethanol. The solutions obtained are in general colourless and transparent. When exposed to sunlight, they develop a strong coloration and regain the colourless state when they are placed in an area of less exposure to the sun's rays or, in other words, when they are no longer submitted to UV. In general, a very low concentration of product (of the order of 0.01 to 5% by weight) is sufficient to obtain an intense coloration.
The compounds according to the invention are furthermore compatible with support matrices of organic polymer or of inorganic material, in a form included in said matrices as well as in the form of a coating of said matrices.
Also, within the context of the fourth aspect of the invention in relation to the photochromic applications, the object of the invention is a matrix which comprises:
at least one compound (I), as defined supra;
and/or at least one (co)polymer and/or reticulate, as defined supra;
and/or at least one composition, as presented above.
The most interesting applications of the compounds of the invention are in fact those in which the photochrome is dispersed uniformly within or on the surface of a matrix formed by a polymer and/or copolymer and/or mixture of (co)polymers.
Following the example of their behaviour in solution, the compounds (I), included in a polymer matrix are colourless or slightly coloured in the initial state and rapidly develop an intense coloration under a UV light (365 nm) or under a light source of the solar type. Finally, they regain their initial coloration once the irradiation ceases.
The methods of implementation which can be envisaged in order to obtain such a matrix are very varied. Amongst those known to the person skilled in the art, the diffusion in the (co)polymer, from a suspension or solution of the photochrome, in a silicone oil, in an aliphatic or aromatic hydrocarbon, or in a glycol, or from another polymer matrix, can be cited for example. The diffusion is commonly carried out at a temperature of 50 to 200° C. for a period of time of 15 minutes to several hours, according to the nature of the polymer matrix. Another implementation technique consists in mixing the photochrome in a formulation of polymerisable matrices, depositing this mixture on a surface or in a mould, and then carrying out the copolymerisation. These implementation techniques, and others, are described in the article by Crano et al. “Spiroxazines and their use in photochromic lenses” published in Applied Photochromic Polymer Systems, Ed. Blackie and Son Ltd—1992.
The following products may be mentioned as examples of preferred polymer materials for forming matrices which are useful in optical applications of the photochromic compounds according to the invention:
alkyl, cycloalkyl, (poly or oligo)ethylene glycol, aryl or arylalkyl mono-, di- tri- or tetraacrylate or mono-, di-, tri- or tetramethacrylate, which is optionally halogenated or which comprises at least one ether and/or ester and/or carbonate and/or carbamate and/or thiocarbamate and/or urea and/or amide group,
polystyrene, polyether, polyester, polycarbonate (e.g. bisphenol-A polycarbonate, diallyl diethylene glycol polycarbonate), polycarbamate, polyepoxy, polyurea, polyurethane, polythiourethane, polysiloxane, polyacrylonitrile, polyamide, aliphatic or aromatic polyester, vinylic polymers, cellulose acetate, cellulose triacetate, cellulose acetate-propionate or polyvinylbutyral,
those obtained from difunctional monomers having the formula below:
R10, R′10, R11 and R′11 are identical or different and represent independently a hydrogen or a methyl group;
m1 and n1 are, independently, integers between 0 and 4 (inclusive); and are advantageously independently equal to 1 or 2;
X and X′, which are identical or different, are a halogen and represent, preferably, a chlorine and/or a bromine;
p1 and q1 are, independently, integers between 0 and 4 (inclusive);
copolymers of at least two types of copolymerisable monomers selected from the precursor monomers of the polymers listed supra, and preferably those belonging to the groups comprising: (meth)acrylic monomers, vinylic monomers, allylic monomers, and mixtures thereof.
In a particularly preferred manner, the photochromes of the invention are used with resins which have a nanobiphasic structure and which are obtained by copolymerising at least two different, specific difunctional monomers. Such resins have been described by the Applicant in the French patent Application FR-A-2,762,845.
The amount of photochrome used in the (co)polymer matrix depends upon the degree of darkening desired. Usually, between 0.001 and 20% by weight of it is used.
Still according to the fifth of its aspects in relation to the applications of the compounds (I) as photochromes, another object of the present invention is ophthalmic articles, such as ophthalmic or solar spectacle articles, comprising:
at least one compound (I) according to the invention,
and/or at least one (co)polymer and/or reticulate formed, at least in part, from compound(s) of the invention,
and/or at least one photochromic composition as defined above,
and/or at least one matrix (as defined supra), of an organic polymer material or of an inorganic material, or even of a hybrid inorganic-organic material, said matrix initially optionally comprising at least one compound of the invention.
In practice, the articles which are more particularly covered by the present invention are ophthalmic lenses or photochromic solar lenses, glazing (windows for buildings, for locomotion engines, automobile vehicles), optical devices, decorative articles, solar protection articles, information storage, . . .
The present invention is illustrated by the Examples which follow of synthesis and of photochromic validation, of compounds of the invention. Said compounds of the invention are compared to prior art compounds C1, C2 and C3.
The synthesis of compound (1) was carried out according to route A described supra.
In a 250 ml conical flask, the following products are loaded in the order: 40 ml of THF, 33.5 ml of PhMgBr (3M ether) and 3.4 g of CuI. The mixture is cooled to −30° C., and a solution of 10 g of epoxynorbornane in 50 ml of THF is then poured in. After 30 minutes at 30° C., the temperature is allowed to rise to 25° C. and after 16 hours, the medium is poured into an ammonium chloride solution. The organic phase is recovered, washed with 3×150 ml of an ammonium chloride solution, and then dried over magnesium sulphate. 12.5 g of an oil are recovered which contains the desired product.
In a 500 ml conical flask, the following products are loaded in the order: 11.5 g of the product of the preceding step, 200 ml of dichloromethane, 60 g of Celite and 39 g of pyridinium chlorochromate. After 1.5 hours at ambient temperature, 200 ml diisopropyl ether are poured into the medium and the suspension is filtered. After evaporation to dryness, 12 g of a brown liquid are recovered that is purified by chromatography on silica in eluting with a toluene/dichloromethane 80/20 mixture. 5.84 g of the desired product are recovered in the form of an oil.
In a 250 ml conical flask equipped with a Dean-Stark collector, the following mixture: 5.85 g of the product of the preceding step, 3.55 g of ethyl cyanoacetate, 2.7 g of ammonium acetate, 2.2 g of acetic acid and 100 ml of toluene, is heated under reflux for 24 hours. 10 g of acetamide are then added and the toluene is distilled off. After 6 hours at 200-220° C., the medium is poured into 300 ml of water, and the product is then extracted with a THF/ethyl acetate mixture. The product is then purified by chromatography on silica in eluting with a toluene/dichloromethane 60/40 mixture. 1.37 g of the desired intermediate product are isolated after recrystallisation.
The following mixture 1.37 g of the product of the preceding step, 2.7 g of KOH in 15 ml of n-butanol, is heated at about 200-220° C. for 6 hours in a 125 ml acid digestion bomb. After cooling, the mixture is transferred into a flask and is then reduced to dryness. The paste is then dissolved in 50 ml of water and is then neutralised by the slow and progressive addition of concentrated hydrochloric acid. The product is extracted with 60 ml of diisopropyl ether, washed with 2×100 ml of water and then dried over magnesium sulphate. After evaporation to dryness, 1.3 g (98%) of a brown oil are recovered.
The following mixture: 0.5 g of the product of the preceding step, 0.78 g 1,1-bis(para-methoxyphenyl)propyne-1-ol in 10 ml of dichloromethane, is heated under reflux in the presence of a catalytic amount of bromoacetic acid in a 100 ml reactor for 5 hours. The product is then purified by chromatography on silica in eluting with toluene. The purest fractions are combined which are reduced to dryness. About 50 mg of the desired photochrome are obtained. Its structure is confirmed by NMR spectroscopy.
The synthesis of compound (2) was carried out according to route A described supra.
The method is analogous to that described for the compound of Example 1 in starting from the 1-bromonaphthalene Grignard reagent instead of the bromobenzene Grignard reagent. In step 4, the following mixture: 0.35 g of the phenanthrol originating from step 3 and 1.2 g of 1,1-bis(para-methoxyphenyl)propyn-1-ol in 15 ml of toluene is heated under reflux in the presence of a catalytic amount of bromoacetic acid for 4 hours. The product is then purified by chromatography on silica in eluting with a toluene/heptane 80/20 mixture. The purest fractions are combined and are reduced to dryness. A recrystallisation in a toluene/heptane mixture at 0° C. enables isolating about 50 mg of the desired photochrome. Its structure is confirmed by NMR spectroscopy.
The method is analogous to that described for the preceding product. In step 4, the following mixture: 0.35 g of the phenanthrol originating from step 3 and 1.2 g of 1-phenyl-1-(para-dimethylaminophenyl)-propyn-1-ol in 15 ml of toluene is heated under reflux in the presence of a catalytic amount of bromoacetic acid for 14 hours. The product is then purified by chromatography on silica in eluting with a toluene/heptane 80/20 mixture. The purest fractions are combined and are reduced to dryness. A recrystallisation in a toluene/heptane mixture at 0° C. enables isolating about 50 mg of the desired photochrome. Its structure is confirmed by NMR spectroscopy.
The synthesis of compound (4) was carried out according to route A described supra.
The method is analogous to that described for the compound of Example 1 in starting from the 2-bromonaphthalene Grignard reagent instead of the bromobenzene Grignard reagent. In step 4, the following mixture: 0.7 g of the phenanthrol originating from step 3 and 1.0 g of 1-(para-methoxyphenyl)-1-(para-dimethylaminophenyl)propyn-1-ol in 15 ml of toluene is heated under reflux in the presence of a catalytic amount of bromoacetic acid for 7 hours. The product is then purified by chromatography on silica in eluting with a toluene/heptane 70/30 mixture.
The purest fractions are combined and are reduced to dryness. A recrystallisation in a toluene/heptane mixture at 0° C. enables isolating about 140 mg of the desired photochrome. Its structure is confirmed by NMR spectroscopy.
Compound C1 is commercially available. Compounds C2 and C3 are described in the U.S. Pat. No. 5,783,116 patent.
The photochromic properties of said compounds (1), (2), (3), (4), C1, C2 and C3 were evaluated.
Said compounds are dissolved, at the rate of 5 mg in 50 ml of THF. The UV-visible absorptions (optical path of 1 cm) are then measured before and after exposure to a 365 nm UV source. The observation of the tints and intensities developed is made by placing the solutions in the sun or before a solar simulator. The properties of these compounds are given in the Table below.
*λ1 max of the band of the longest wavelength of the compound before exposure.
**λ2 max of the band of the longest wavelength of the compound after exposure.
The observation of the solutions in the presence of solar or UV rays shows that the compounds of the invention have λ1 and λ2 which are shifted towards longer wavelengths (bathochromic shift). This observation is especially evident by comparing the λmax's of the compound (1) with the analogous compounds C1, C2 and C3.
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|WO1997021698A1||Dec 12, 1996||Jun 19, 1997||Ppg Industries Inc||Novel substituted naphthopyrans|
|U.S. Classification||568/733, 568/632, 560/64, 564/172, 560/56, 568/634, 564/308|
|International Classification||C08F8/00, C08G85/00, C09K9/02, C07C39/17, C07D311/94, C07D311/92, C08K5/1545, C07D311/78, G02B5/23|
|Cooperative Classification||G02B5/23, C07D311/78, C07D311/92, C07D311/94, C08K5/1545|
|European Classification||C07D311/92, C07D311/78, C08K5/1545, G02B5/23, C07D311/94|
|Mar 3, 2006||FPAY||Fee payment|
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|Mar 3, 2014||FPAY||Fee payment|
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